Ll-miRn1 |
TTGCCAATTCCACCCATGCCTA |
22 |
TRINITY_DN58100_c0_g3_i1 |
125 |
−59.90 |
SUPPRESSOR OF GENE SILENCING 3
|
Ll-miRn2 |
TCACTCCAACTTTGACCTTCT |
21 |
TRINITY_DN50576_c0_g2_i1 |
215 |
−84.70 |
65-kDa microtubule-associated protein 7
|
Ll-miRn3 |
TGAAGAGGGAGGGAGACTGATG |
22 |
TRINITY_DN77107_c0_g1 |
185 |
−86.50 |
SRC2 homolog
|
Ll-miRn4 |
GTAGCACCATCAAGATTCACA |
21 |
TRINITY_DN43941_c0_g1_i1 |
151 |
−60.30 |
RCC1 and BTB domain-containing protein 2 |
Ll-miRn5 |
TGGAATAGTGAATGAGACATC |
21 |
TRINITY_DN52736_c3_g2_i2 |
102 |
−38.70 |
Probable cinnamyl alcohol dehydrogenase 9 |
Ll-miRn6 |
TGCTATCCATCCTGAGTTTCA |
21 |
TRINITY_DN54182_c6_g1_i1 |
133 |
−47.90 |
Probable amino acid permease 7 |
Ll-miRn7 |
AGAGGTGTATGGCACAAGAGA |
21 |
TRINITY_DN53175_c1_g6_i1 |
85 |
−36.60 |
Probable protein phosphatase 2C |
Ll-miRn8 |
TGAAGTGTTTGGGGGAACTCC |
21 |
TRINITY_DN44441_c0_g1_i1 |
102 |
−37.40 |
ATP sulfurylase 1
|
Ll-miRn9 |
TCGGACCAGGCTTTATTCCTT |
21 |
TRINITY_DN50586_c0_g1_i3 |
167 |
−65.60 |
Homeobox-leucine zipper protein REVOLUTA
|
Ll-miRn10 |
ATGTTGTGATGGGAATCAATG |
21 |
TRINITY_DN67022_c0_g1_i1 |
84 |
−43.50 |
CBL-interacting serine/threonine-protein kinase 6
|
Ll-miRn11 |
TAAAGACCTCATTCTCTCATG |
21 |
TRINITY_DN31556_c0_g1_i1 |
130 |
−62.80 |
Vacuolar protein sorting-associated protein 62
|
Ll-miRn12 |
AGGTCATCTTGCAGCTTCAAT |
21 |
TRINITY_DN52990_c2_g1_i5 |
71 |
−36.84 |
DNA-directed RNA polymerase I subunit 1 |
Ll-miRn15 |
TTCGGCTTTCTACTTCTCATG |
21 |
TRINITY_DN54101_c8_g2_i10 |
156 |
−66.20 |
Transcription termination factor MTERF8
|
Ll-miRn16 |
AGTTCTTTAGATGGGCTGGACGCC |
24 |
TRINITY_DN52523_c6_g2_i1 |
83 |
−36.50 |
Amino acid transporter AVT6A |
Ll-miRn17 |
TGTCTCATTCTCTATCTCAAG |
21 |
TRINITY_DN51068_c0_g1_i2 |
142 |
−64.30 |
IST1-like protein |
Ll-miRn18 |
AATAGGGCACATCTCTCATGG |
22 |
TRINITY_DN46596_c0_g1_i1 |
112 |
−49.00 |
E3 ubiquitin-protein ligase HOS1 |
Ll-miRn19 |
TCCAAAGGGATCGCATTGATTT |
22 |
TRINITY_DN53637_c4_g2_i4 |
110 |
−48.10 |
AUXIN SIGNALING F-BOX 3
|
Ll-miRn21 |
TGAGCATGAGGATAAGGACGG |
21 |
TRINITY_DN50271_c0_g3_i1 |
246 |
−144.90 |
Tetratricopeptide repeat protein 1
|
Ll-miRn22 |
TATCATTCCATACATCGTCTCG |
21 |
TRINITY_DN50592_c0_g4_i2 |
80 |
−33.60 |
Putative disease resistance RPP13-like protein 1 |
Ll-miRn24 |
ATTGTCACTGTATCATTCACCATT |
24 |
TRINITY_DN52987_c0_g1_i1 |
104 |
−32.30 |
Zinc finger CCCH domain-containing protein 55 |
Ll-miRn25 |
TGGTACAAAAAGTGGGGCAAC |
21 |
TRINITY_DN48871_c3_g1_i9 |
151 |
−43.90 |
Nuclear transcription factor Y subunit A-9 |
Ll-miRn26 |
TGTTGTTTTCTGGTAAAAATA |
21 |
TRINITY_DN58488_c1_g2_i4 |
99 |
−33.80 |
Auxin-responsive protein IAA27 |
Ll-miRn27 |
ATTAGATCATGTGGCAGTTTCACC |
24 |
TRINITY_DN51506_c3_g2_i5 |
77 |
−36.60 |
U-box domain-containing protein 33 |
Ll-miRn28 |
TACGGGTGTCCTCACCTCTGAT |
22 |
TRINITY_DN70730_c0_g1_i1 |
98 |
−36.90 |
ISWI chromatin-remodeling complex ATPase
|
Ll-miRn29 |
TGGGATAGAGAGTGAGATACC |
21 |
TRINITY_DN51068_c0_g1_i2 |
125 |
−67.80 |
Ethylene-responsive transcription factor ERF017 |
Ll-miRn30 |
TTCGTTTGTGTGCAGACTCTGT |
22 |
TRINITY_DN57730_c1_g9_i2 |
105 |
−42.70 |
Endoribonuclease Dicer homolog 2
|
Ll-miRn31 |
GCGTACCAGGAGCCATGCATG |
21 |
TRINITY_DN58934_c0_g4_i1 |
149 |
−60.20 |
Calcium-transporting ATPase 4 |
Ll-miRn32 |
AAGGGTTGTTTACAGAGTTTA |
21 |
TRINITY_DN51330_c0_g1_i1 |
128 |
−55.40 |
26S proteasome regulatory subunit 7 |